A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844579



Internal ID22619514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24804297..24806501hg38UCSC Ensembl
chr6:24804525..24806729hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504368
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844579
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer